US3793400A - Polyester-1,2 polybutadiene high impact molding compound - Google Patents

Polyester-1,2 polybutadiene high impact molding compound Download PDF

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US3793400A
US3793400A US00189005A US3793400DA US3793400A US 3793400 A US3793400 A US 3793400A US 00189005 A US00189005 A US 00189005A US 3793400D A US3793400D A US 3793400DA US 3793400 A US3793400 A US 3793400A
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polyester
polybutadiene
weight
acid
molding
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O Curtis
C Mason
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Honeywell International Inc
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Allied Chemical Corp
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/06—Unsaturated polyesters

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  • This invention relates to improved unsaturated polyester molding compositions. More particularly, this invention relates to certain unsaturated polyester molding compositions containing certain 1,2-polybutadiene resins which have improved impact resistance.
  • Alkyd molding compositions are well known and are prepared from unsaturated polyesters of unsaturated aliphatic dibasic carboxylic acids and glycols admixed with fillers, lubricants, stabilizers, and peroxide curing agents. Alkyd molding compositions are inexpensive and can be readily fabricated by high speed, automatic equipment for a variety of products including automotive ignition components, switch gear components, and the like.
  • alkyd resins have one disadvantage, inadequate toughness, which has limited their large scale use for example in the automotive industry, wherein molded parts must be able to withstand multi-step handling, machining, and processing with no long-term loss of strength.
  • High performance plastics such as phenolics are presently preferred by the industry. However, phenolics have poor electrical properties, particularly at elevated temperatures, whereas alkyd resins have excellent electrical properties. Thus an alkyd resin having improved toughness would be highly desirable for molded parts for electrical and other components.
  • molding compositions of certain unsaturated polyesters, containing certain 1,2-polybutadiene resins can be utilized in alkyd molding compositions which, when cured, exhibit greatly improved impact resistance and toughness and have high heat distortion temperatures.
  • the alkyd molding compositions of the invention are derived from an unsaturated polyester having a high fumarate functionality of at least about 55%, preferably 60-78%, by weight of the polyester, a glycol and optionally an aromatic dibasic carboxylic acid, admixed with from 3-20% by weight of the molding composition, preferably 5-15% by weight, of a l,2-'polybutadiene resin having a high 1,2-vinyl content of at least 70%, preferably 70-95 by weight of the butadiene polymer and conventional fillers, catalysts, inhibiters, and the like.
  • the unsaturated polyesters useful in the invention are the reaction products of fumaric and/or maleic acid or their anhydrides, with a glycol, and when required, also an aromatic dibasic acid.
  • the unsaturated polyesters must have a fumarate functionality, that is, the percentage by weight of unsaturated acid calculated as fumaric acid, of at least 55% and preferably from 60-78%.
  • a fumarate functionality that is, the percentage by weight of unsaturated acid calculated as fumaric acid, of at least 55% and preferably from 60-78%.
  • the polyester has a high fumarate functionality, e.g., over about no aromatic dibasic acid need be added.
  • an amount of aromatic acid required to dilute the functionality to the desired level is also added.
  • Suitable aromatic dibasic acids include phthalic acid, isophthalic acid, terephthalic acid, trimellitic acid, and the like, or their anhydrides. Isophthalic acid is preferred for high impact materials.
  • Glycols suitable for preparing the polyesters include aliphatic diols such as ethylene glycol, propylene glycol, 1,2-, 1,3-, 1,4-butane diols, 1,6-hexane diol, diethylene glycol, triethylene glycol, dipropylene glycol, and the like; and aromatic diols, such as bis[4-(2-hydroxy)propoxyphenyl]dime-thylmethane and the like. Mixtures of glycols can also be employed.
  • aliphatic diols such as ethylene glycol, propylene glycol, 1,2-, 1,3-, 1,4-butane diols, 1,6-hexane diol, diethylene glycol, triethylene glycol, dipropylene glycol, and the like
  • aromatic diols such as bis[4-(2-hydroxy)propoxyphenyl]dime-thylmethane and the like. Mixtures of glycols can also be employed.
  • the unsaturated polyester generally contains an inhibiter to prevent premature curing or cross-linking.
  • Suitable inhibiters are well known and include hydroquinone, mono-t-butylhydroquinone, t-butyl catechol, tetrachloroquinone, and the like.
  • the 1,2-polybutadienes suitable for use in the invention must have a 1,2-vinyl content of at least about 70%, preferably 70-95%, by weight of the resin.
  • Polybutadienes having a molecular weight of about 100,000-300,000 are 'preferred in the invention.
  • lower molecular weight resins having a molecular weight in the range 10,000-100,000 can also be employed when admixed, in amounts up to 50% by weight of the 1,2-polybutadiene, with 1,4-polybutadiene having a high molecular weight, i.e. over 100,000.
  • the presence of excessive amounts of 1,4-polybutadiene has a deleterious effect on the heat distortion temperature of the resultant cured polyesters.
  • the molding compositions of the invention are prepared by admixing the unsaturated polyesters, the 1,2- polybutadiene resin (both as hereinabove described), and other conventional ingredients such as monomers, if employed, catalysts, fillers, and pigments.
  • HDT high temperature
  • the dropping ball impact test is carried out as follows:
  • a cross-linking monomer is not required to 5 a 66.75 gm. ball is dropped onto molded 4 x A3" discs of cure the molding compositions of the invention
  • a monothe molding resin initially from a height of 6 inches, and mer can be added to aid in cross-linking the unsaturated thereafter at two inch intervals more, until the disc cracks polyesters as is known.
  • the addition of a cross-linking or breaks. Results are reported in inches corresponding monomer generally improves the melt flow and proces- 10 to the height at which cracking or breaking occurs. ThlS sability of the resin. Suitable monomers contain a test is described in Canadian Pat. 759,096,
  • -CH C group and include styrene, ethyl-a-methylstyrene, chloroand fluorostyrenes, vinyl toluene, divinyl EXAMPLE 1 benzene, diallyl maleate, methallyl maleate, allyl suocinyl,
  • Suitable catalysts for the molding compositions of the ig g g i g zi fg f invention are also well known and include peroxides such f an G 1 1;: e i f L to as benzoyl peroxide, t-butyl perbenzoate, lauroyl peroxide, z gg f 2 g f f Solution of dicumyl peroxide, 2,5-dirnethyl 2,5 bis(benzoylperoxy) hexane, isopropylbenzene hydroperoxide, methyl ethyl kezlydrocglmomzf m 1 .g
  • the preferred catalysts are dicumyl peroxide and 2,5-dimethyl-2,5-bis(benzoylperoxy)hexane.
  • Catalysts are (B) Prepammn of moldmg gelqsrally employed amounts of Q to 5% by Molding compositions were prepared by admixing the weight of the unsaturated polyester. Mixtures of catalysts polyester as Prepared above with a 1,2.pO1ybu/[adiene can also be p y resin having 70% of 1,2-vinyl content and a molecular The unsaturated polyester resins generally also contain 40 weight of 250,000-300,000. The 1,2-polybutadiene was inhibiters to improve shelf life. Illustrative of known omitted from the control.
  • the blends were admixed with inhibiters are t-butyl catechol, hydroquinone and t-butylabout 75% of a calcium carbonate filler, about 0.25% of hydroquinone. zinc stearate, about 1.25% of dicumyl peroxide, and about Fillers suitable for preparation of the present molding 0.001% of Lignocol, a phenolic inhibiter of Heyden Newcompositions are well known and include organic and port Chemical Corporation, and blended for ten minutes. inorganic fillers such as oz-CellulOSC, glass fibers, clay, The above proportions are percentages based on the total asbestos, silica, calcium carbonate, zinc oxide, and the weight of. the mixture. These blends were then passed like.
  • Gardner-Holdt viscosity was determined according to ASTM test Dl54-64, acid number according to ⁇ ASTM test D1639-61, heat distortion It is apparent that the addition of 1,2-polybutadiene greatly improves the impact resistance of the alkyd molding resin with no decrease in flexural strength, while retaining a high heat distortion temperature.
  • the molding compositions of the invention also produce articles having improved electrical properties as shown by the following results:
  • Example 1 The procedure of Example 1, Run 4 was followed except substituting for the filler 75% by weight of the molding composition of silica and 0.3% of gamma-methacryloxypropyltrimethoxysilane.
  • Polyester percent Flexural 19 3- -p y- Dropping butadlene, butadlene, HDT, ball impact, Strength, Modulus, percent percent 0. in. p.s.i. p.s.i. X10- Dropping ball impact was 18 in., flexural strength 11,260 p.s.i., flexural modulus 142 10 p.s.i. and -I-IDT 142 C.
  • Example 5 The procedure of Example 1 was followed except substituting for the fumarate polyester a polyester of maleic anhydride, isophthalic acid and ethylene glycol, having a calculated fumarate functionality of 63%. Results are given below:
  • Example 7 The procedure of Example 1 was followed except substituting for the 1,2-polybutadiene resin a 1,2-polybutadiene polymer having a molecular weight of only 13,000.
  • An alkyd molding composition comprising an unsaturated polyester derived from a dibasic aliphatic acid selected from the group consisting of fumaric acid, maleic acid or their anhydrides and a glycol, the polyester having a fumarate functionality of from 55 to about 78% by weight of the polyester, and from 3 to about 20% by weight of the molding composition of polybutadiene which is a polybutadiene having a 1,2-vinyl content of at least about and a molecular weight of from about 100,000 to about 300,000, or a blend of 1,2-polybutadiene having a 1,2-vinyl content of at least about 70% and a molecular weight of from about 10,000 to about 100,000 with up to an equal amount of 1,4-polybutadiene having a molecular weight over 100,000.
  • polybutadiene which is a polybutadiene having a 1,2-vinyl content of at least about and a molecular weight of from about 100,000 to about 300,000, or a blend of 1,2-polybut
  • composition according to claim 1 wherein the polyester has a fumarate functionality of 60-78% by weight of the polyester.
  • composition according to claim 1 wherein the polyester is derived from fumaric acid or maleic anhydride, an aromatic dibasic acid, and one or more glycols.
  • polybutadiene is a polybutadiene having a 1,2-vinyl content of at least about 70% and a molecular weight of from about 100,000 to about 300,000.
  • polybutadiene is a blend of 1,2-polybutadiene having a 1,2-vinyl content of at least about 70% and a molecular weight from about 10,000 to about 100,000 with up to an equal amount of a 1,4-polybutadiene having a molecular weight over 100,000.
  • a composition according to claim 1 additionally containing a filler.
  • a high impact alkyd molding composition comprising an unsaturated polyester derived from an aliphatic dibasic acid selected from the group consisting of fumaric acid, maleic acid or their anhydrides, a glycol and an aromatic dibasic acid, the polyester having a fumarate functionality of from 55 to about 78% by Weight of'the polyester and from about 5 to about 15% by weight of the molding composition of a 1,2-polybutadiene having a 1,2- vinyl content of from 70 to 95% by weight of the polybutadiene polymer and a molecular weight of from about 100,000 to about 300,000.
  • composition according to claim 8 wherein the aromatic dibasic acid is isophthalic acid.
  • composition according to claim 8 wherein the polyester has a fumarate functionality of at least about 60%.
  • a composition according to claim 8 additionally containing a filler.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
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Abstract

THE ADDITION OF CERTAIN 1,2-POLYBUTADIENE RESINS TO UNSATURATED POLYESTERS IMPROVES IMPACT RESISTANCE AND TOUGHNESS WITH NO LOSS OF HEAT DISTORTION TEMPERATURE.

Description

United States Patent 3,793,400 POLYESTER-1,2 POLYBUTADIENE HIGH IMPACT MOLDING COMPOUND Omer Eugene Curtis, Jr., Morristown, and Charles Driscoll Mason, Florham Park, N.J., assignors to Allied Chemical Corporation, New York, N.Y. No Drawing. Filed Oct. 13, 1971, Ser. No. 189,005
Int. Cl. 008g 39/10, 51/04, 51/18 US. Cl. 260-862 14 Claims ABSTRACT OF THE DISCLOSURE The addition of certain 1,2-polybutadiene resins to unsaturated polyesters improves impact resistance and toughness with no loss of heat distortion temperature.
This invention relates to improved unsaturated polyester molding compositions. More particularly, this invention relates to certain unsaturated polyester molding compositions containing certain 1,2-polybutadiene resins which have improved impact resistance.
BACKGROUND OF THE INVENTION Alkyd molding compositions are well known and are prepared from unsaturated polyesters of unsaturated aliphatic dibasic carboxylic acids and glycols admixed with fillers, lubricants, stabilizers, and peroxide curing agents. Alkyd molding compositions are inexpensive and can be readily fabricated by high speed, automatic equipment for a variety of products including automotive ignition components, switch gear components, and the like. However, alkyd resins have one disadvantage, inadequate toughness, which has limited their large scale use for example in the automotive industry, wherein molded parts must be able to withstand multi-step handling, machining, and processing with no long-term loss of strength. High performance plastics such as phenolics are presently preferred by the industry. However, phenolics have poor electrical properties, particularly at elevated temperatures, whereas alkyd resins have excellent electrical properties. Thus an alkyd resin having improved toughness would be highly desirable for molded parts for electrical and other components.
DISCUSSION OF THE PRIOR ART The addition of a rubbery component to a thermoplastic resin to improve impact resistance and toughness is known, but addition of such materials to thermoplastic molding compositions does not always impart added toughness.
US. Pat. 3,231,634 to Wismer et al., teaches that unsaturated polyester resins can be modified by blending with a rubbery polymer to impart cracking resistance. The rubbery polymers added are polymers of conjugated dienes, such as butadiene, isoprene, haloprene, and copolymers thereof. However, the cured compositions of Wismer et a1. exhibit a marked decrease in heat distortion temperature. This is unacceptable since the heat distortion temperature determines the temperature at which the composition can be molded without deformation of the article upon ejection from the mold. If the molding temperature is too low, the molding cycle time must be increased, with corresponding increase in cost. Further, the heat distortion temperature determines the temperature at which the mechanical and electrical properties of the cured resin deteriorate rapidly, thus defining its upper use temperature.
SUMMARY OF THE INVENTION It is an object of the present invention to provide alkyd resin compositions having improved toughness.
It is a further object to provide molding compositions "ice which can be formed and cured into tough molded articles having high heat distortion temperatures and excellent electrical properties.
Further objects will become apparent from the following detailed description thereof.
It has been discovered that molding compositions of certain unsaturated polyesters, containing certain 1,2-polybutadiene resins can be utilized in alkyd molding compositions which, when cured, exhibit greatly improved impact resistance and toughness and have high heat distortion temperatures.
The alkyd molding compositions of the invention are derived from an unsaturated polyester having a high fumarate functionality of at least about 55%, preferably 60-78%, by weight of the polyester, a glycol and optionally an aromatic dibasic carboxylic acid, admixed with from 3-20% by weight of the molding composition, preferably 5-15% by weight, of a l,2-'polybutadiene resin having a high 1,2-vinyl content of at least 70%, preferably 70-95 by weight of the butadiene polymer and conventional fillers, catalysts, inhibiters, and the like. Conventional cross-linking monomers containing a CH =C group can also be added.
DETAILED DESCRIPTION OF THE INVENTION The unsaturated polyesters useful in the invention are the reaction products of fumaric and/or maleic acid or their anhydrides, with a glycol, and when required, also an aromatic dibasic acid.
The unsaturated polyesters must have a fumarate functionality, that is, the percentage by weight of unsaturated acid calculated as fumaric acid, of at least 55% and preferably from 60-78%. When the polyester has a high fumarate functionality, e.g., over about no aromatic dibasic acid need be added. When a lower functionality resin is desired, an amount of aromatic acid required to dilute the functionality to the desired level is also added.
Suitable aromatic dibasic acids include phthalic acid, isophthalic acid, terephthalic acid, trimellitic acid, and the like, or their anhydrides. Isophthalic acid is preferred for high impact materials.
Glycols suitable for preparing the polyesters include aliphatic diols such as ethylene glycol, propylene glycol, 1,2-, 1,3-, 1,4-butane diols, 1,6-hexane diol, diethylene glycol, triethylene glycol, dipropylene glycol, and the like; and aromatic diols, such as bis[4-(2-hydroxy)propoxyphenyl]dime-thylmethane and the like. Mixtures of glycols can also be employed.
The unsaturated polyester generally contains an inhibiter to prevent premature curing or cross-linking. Suitable inhibiters are well known and include hydroquinone, mono-t-butylhydroquinone, t-butyl catechol, tetrachloroquinone, and the like.
The 1,2-polybutadienes suitable for use in the invention must have a 1,2-vinyl content of at least about 70%, preferably 70-95%, by weight of the resin. Polybutadienes having a molecular weight of about 100,000-300,000 are 'preferred in the invention. However, lower molecular weight resins having a molecular weight in the range 10,000-100,000, can also be employed when admixed, in amounts up to 50% by weight of the 1,2-polybutadiene, with 1,4-polybutadiene having a high molecular weight, i.e. over 100,000. However, the presence of excessive amounts of 1,4-polybutadiene has a deleterious effect on the heat distortion temperature of the resultant cured polyesters.
The molding compositions of the invention are prepared by admixing the unsaturated polyesters, the 1,2- polybutadiene resin (both as hereinabove described), and other conventional ingredients such as monomers, if employed, catalysts, fillers, and pigments.
manner as will be known to one skilled in the art. The
manner and order of mixing of the ingredients of the present molding compositions are not critical and do not alfect the properties of the resultant cured polymer.
temperature (hereinafter HDT) according to ASTM test D648, Izod Impact according to ASTM test D256-56, and flexural strength and flexural modulus according to ASTM test D790.
The dropping ball impact test is carried out as follows:
Although a cross-linking monomer is not required to 5 a 66.75 gm. ball is dropped onto molded 4 x A3" discs of cure the molding compositions of the invention, a monothe molding resin, initially from a height of 6 inches, and mer can be added to aid in cross-linking the unsaturated thereafter at two inch intervals more, until the disc cracks polyesters as is known. The addition of a cross-linking or breaks. Results are reported in inches corresponding monomer generally improves the melt flow and proces- 10 to the height at which cracking or breaking occurs. ThlS sability of the resin. Suitable monomers contain a test is described in Canadian Pat. 759,096,
-CH =C group and include styrene, ethyl-a-methylstyrene, chloroand fluorostyrenes, vinyl toluene, divinyl EXAMPLE 1 benzene, diallyl maleate, methallyl maleate, allyl suocinyl,
allyl glycolate, bis(allyacetate)digycolate, diallyl phenyl 5 (A) Preparatlon of Poll/fister hos honate, diallyl phthalate, methyl methacrylate,
grow 1 acrylate, butyl acrylate, vinyl acetate, allyl To a resm g, gf i Surfer gas $3 acetate, tris-(Z-hydroxyethyl)isocyanurate, triallyl iS(l)Cy' igi g z gg ir i '6 i g r o i i bph zli acid 1562 anurate, triall l c anurate, diall l itaconate, meth ene the my mime a extras:11221.12 .a a ir.si. itsgsrztsis usually employed in amounts of up to 5% by weight While stimn g, the temperature was increased over a two co umn remame e ow e is a on E ESZz ZE Z ZEF the resultant cured resms have lower was removed after one hour and heating continued for Suitable catalysts for the molding compositions of the ig g g i g zi fg f invention are also well known and include peroxides such f an G 1 1;: e i f L to as benzoyl peroxide, t-butyl perbenzoate, lauroyl peroxide, z gg f 2 g f f Solution of dicumyl peroxide, 2,5-dirnethyl 2,5 bis(benzoylperoxy) hexane, isopropylbenzene hydroperoxide, methyl ethyl kezlydrocglmomzf m 1 .glycol was g i and q tone peroxide, cyclohexanone peroxide, acetyl benzoyl or a fii i' resmt 2 l g peroxide, hydroxyheptyl peroxide, p-chlorobenzoyl peroxgeratuye' e p0 yas er con ame 0 y welg ide, peracetic acid, acetyl peroxide, t-butyl peracetate and mane am the like. The preferred catalysts are dicumyl peroxide and 2,5-dimethyl-2,5-bis(benzoylperoxy)hexane. Catalysts are (B) Prepammn of moldmg gelqsrally employed amounts of Q to 5% by Molding compositions were prepared by admixing the weight of the unsaturated polyester. Mixtures of catalysts polyester as Prepared above with a 1,2.pO1ybu/[adiene can also be p y resin having 70% of 1,2-vinyl content and a molecular The unsaturated polyester resins generally also contain 40 weight of 250,000-300,000. The 1,2-polybutadiene was inhibiters to improve shelf life. Illustrative of known omitted from the control. The blends were admixed with inhibiters are t-butyl catechol, hydroquinone and t-butylabout 75% of a calcium carbonate filler, about 0.25% of hydroquinone. zinc stearate, about 1.25% of dicumyl peroxide, and about Fillers suitable for preparation of the present molding 0.001% of Lignocol, a phenolic inhibiter of Heyden Newcompositions are well known and include organic and port Chemical Corporation, and blended for ten minutes. inorganic fillers such as oz-CellulOSC, glass fibers, clay, The above proportions are percentages based on the total asbestos, silica, calcium carbonate, zinc oxide, and the weight of. the mixture. These blends were then passed like. through a heated roll mill (front roll 150 F., back roll Additional additives, including mold lubricants, such as 75 F.) a dozen times and formed into a A" thick sheet. zinc stearate, plasticizers, pigments, and dyes can also be The sheets were compression molded at 350 F. for five added to the molding compositions in conventional manminutes at 10,000 p.s.i.g. Physical properties of the resultner, as will be known to one skilled in the art. ant blend are set forth below:
Percent Flexural Dropping Unnotehed Poly- 1,2-poly- HDT, ball Izod Impact, Strength, Modulus, Run number ester butadiene C. impact, in. ft -lbs. p.s.i. p.s.i. X10- The invention will be further illustrated by the following examples, but it is to be understood that the invention is not meant to be limited to the details described therein. In the examples all parts and percentages are by weight unless otherwise noted. Gardner-Holdt viscosity was determined according to ASTM test Dl54-64, acid number according to \ASTM test D1639-61, heat distortion It is apparent that the addition of 1,2-polybutadiene greatly improves the impact resistance of the alkyd molding resin with no decrease in flexural strength, while retaining a high heat distortion temperature.
The molding compositions of the invention also produce articles having improved electrical properties as shown by the following results:
7 Run 1 Run 2 Run 3 Run 4 Room temperature (RT): Dielectric constant (D C)/Dlssipation factor (DF):
60 Hz- 5. 99/. 0072 5. 73/.0050 5. 47/.0053 5.16/.0065 1 kHz 5. 90/. 0064 5. 69/. 0051 5. 43/. 0059 5. 14/. 0051 1 mHz. 5. 89/. 0078 5. 64/. 0070 5. 28/. 0056 175 0.: Dielectric constant (DC)lDissipation factor F):
Hz 8. 99/. 142 7 86/. 191 7. 55/. 190 6. 58/. 129 1 kHz 8. 11/. 0477 7 13/. 0296 6. 76/. 0323 6. 12/. 0211 1 rnHz- 6. 71/. 0143 0. 35/. 0118 5. 76/. 0084 Percent change of RT, DC at 175 C.
60 Hz 50 35 37 30 1 kHz. 37 25 25 20 1 mHz- 15 11 10 Percent change of RT, DF at 175 0.: i 60 Hz- (1, 000 2,800 2,800 1,150 1 kHz 480 420 200 1 mHz 80 69 33 EXAMPLE 2 Results are summarized below:
The procedure of Example 1, Run 4 was followed except substituting for the filler 75% by weight of the molding composition of silica and 0.3% of gamma-methacryloxypropyltrimethoxysilane.
Dropping ball impact was in. and HDT was 220 C.
EXAMPLE 3 Flexural 1,2-poly- Dropping, Polyester, butadiene, HDT, ball impact, Strength, Modulus, percent percent 0. in. p.s.i. p.s.i. X10
Thus, improvement in impact strength is not obtained using low molecular weight polybutadienes alone. However, improved impact can be obtained by addition of higher molecular weight polybutadiene, as is apparent from the results given below:
Polyester, percent Flexural 19 3- -p y- Dropping butadlene, butadlene, HDT, ball impact, Strength, Modulus, percent percent 0. in. p.s.i. p.s.i. X10- Dropping ball impact was 18 in., flexural strength 11,260 p.s.i., flexural modulus 142 10 p.s.i. and -I-IDT 142 C.
EXAMPLE 4 The procedure of Example 1, Run 4 was followed except substituting for the polyester a polyester derived from maleic anhydride and ethylene glycol having a fumarate functionality of 77.5%
Dropping ball impact was 24 in.
EXAMPLE 5 The procedure of Example 1 was followed except substituting for the fumarate polyester a polyester of maleic anhydride, isophthalic acid and ethylene glycol, having a calculated fumarate functionality of 63%. Results are given below:
As a comparison the procedure of Example 1, Run 4 was followed except substituting a polyester having a fumarate functionality of only 47%.
Dropping ball impact was only 14 in.
EXAMPLE 7 The procedure of Example 1 was followed except substituting for the 1,2-polybutadiene resin a 1,2-polybutadiene polymer having a molecular weight of only 13,000.
We claim:
1. An alkyd molding composition comprising an unsaturated polyester derived from a dibasic aliphatic acid selected from the group consisting of fumaric acid, maleic acid or their anhydrides and a glycol, the polyester having a fumarate functionality of from 55 to about 78% by weight of the polyester, and from 3 to about 20% by weight of the molding composition of polybutadiene which is a polybutadiene having a 1,2-vinyl content of at least about and a molecular weight of from about 100,000 to about 300,000, or a blend of 1,2-polybutadiene having a 1,2-vinyl content of at least about 70% and a molecular weight of from about 10,000 to about 100,000 with up to an equal amount of 1,4-polybutadiene having a molecular weight over 100,000.
2. A composition according to claim 1 wherein the polyester has a fumarate functionality of 60-78% by weight of the polyester.
3. A composition according to claim 1 wherein the polyester is derived from fumaric acid or maleic anhydride, an aromatic dibasic acid, and one or more glycols.
4. A composition according to claim 1 wherein the polybutadiene is a polybutadiene having a 1,2-vinyl content of at least about 70% and a molecular weight of from about 100,000 to about 300,000.
5. A composition according to claim 1 wherein the polybutadiene is a blend of 1,2-polybutadiene having a 1,2-vinyl content of at least about 70% and a molecular weight from about 10,000 to about 100,000 with up to an equal amount of a 1,4-polybutadiene having a molecular weight over 100,000.
6. A composition according to claim 1 additionally containing a filler.
7. A composition according to claim 1 additionally containing up to by weight of the total composition of a monomer having a 'CH =C group.
8. A high impact alkyd molding composition comprising an unsaturated polyester derived from an aliphatic dibasic acid selected from the group consisting of fumaric acid, maleic acid or their anhydrides, a glycol and an aromatic dibasic acid, the polyester having a fumarate functionality of from 55 to about 78% by Weight of'the polyester and from about 5 to about 15% by weight of the molding composition of a 1,2-polybutadiene having a 1,2- vinyl content of from 70 to 95% by weight of the polybutadiene polymer and a molecular weight of from about 100,000 to about 300,000.
9. A composition according to claim 8 wherein the aromatic dibasic acid is isophthalic acid.
10. A composition according to claim 8 wherein the polyester has a fumarate functionality of at least about 60%.
11. A composition according to claim 8 additionally containing a filler. 1
12. A molded article of the composition of claim 1.
13. A molded article of the composition of claim 5.
14. A molded article of the composition of claim 8.
References Cited UNITED STATES PATENTS 3,577,478
5/1971 Thorpe 260862 3,714,110 1/ 1973 Verdol et a1. 3,733,370 5/ 1973 Thompson et al.
3,564,077 2/1971 Brinkman et al 260 873 3,598,882 8/1971 Brinkman et al 260873 2,609,353 9/1952 Rubens 260862 2,631,175 3/ 1953 Crouch 260669 3,231,634 1/ 1966 Wismer 260862 3,518,213 6/ 1970 Miyoshi 260862 3,620,900 11/1971 Willinger 161-162 OTHER REFERENCES Kennedy and Torquist, Polymer Chemistry of Synthetic Elastomers, Part II, vol. XXIII, Interscience, 1969, pp. 491 and 564-71. v
WILLIAM H. SHORT, Primary Examiner E. WOODBERRY, Assistant Examiner US. Cl. X.R. 2609, 40 R, 813
US00189005A 1971-10-13 1971-10-13 Polyester-1,2 polybutadiene high impact molding compound Expired - Lifetime US3793400A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3980610A (en) * 1974-11-25 1976-09-14 The Firestone Tire & Rubber Company Unsaturated polyester-1,2 polybutadiene molding compound
US4141863A (en) * 1976-06-11 1979-02-27 Monsanto Company Thermoplastic compositions of rubber and polyester
US4160759A (en) * 1978-01-30 1979-07-10 Exxon Research & Engineering Co. Elastomer modified polyester molding compound
US4205142A (en) * 1977-11-02 1980-05-27 Monsanto Company Flame retardant resin compositions
US4237244A (en) * 1978-01-05 1980-12-02 Bayer Aktiengesellschaft Molding composition based on unsaturated polyesters
US4258147A (en) * 1971-12-23 1981-03-24 General Electric Company Antifoaming resin compositions
US4297389A (en) * 1971-12-23 1981-10-27 General Electric Company Antifoaming resin compositions
WO2012095231A1 (en) * 2011-01-10 2012-07-19 Elantas Gmbh Impregnating resin formulation for electrical windings

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4258147A (en) * 1971-12-23 1981-03-24 General Electric Company Antifoaming resin compositions
US4297389A (en) * 1971-12-23 1981-10-27 General Electric Company Antifoaming resin compositions
US3980610A (en) * 1974-11-25 1976-09-14 The Firestone Tire & Rubber Company Unsaturated polyester-1,2 polybutadiene molding compound
US4141863A (en) * 1976-06-11 1979-02-27 Monsanto Company Thermoplastic compositions of rubber and polyester
US4205142A (en) * 1977-11-02 1980-05-27 Monsanto Company Flame retardant resin compositions
US4237244A (en) * 1978-01-05 1980-12-02 Bayer Aktiengesellschaft Molding composition based on unsaturated polyesters
US4160759A (en) * 1978-01-30 1979-07-10 Exxon Research & Engineering Co. Elastomer modified polyester molding compound
WO2012095231A1 (en) * 2011-01-10 2012-07-19 Elantas Gmbh Impregnating resin formulation for electrical windings
JP2014508194A (en) * 2011-01-10 2014-04-03 エランタス ゲーエムベーハー Impregnating resin formulation for electrical windings
RU2598445C2 (en) * 2011-01-10 2016-09-27 Элантас Гмбх Impregnating resin formulation for electrical windings

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